臺灣學術機構典藏系統 (Taiwan Academic Institutional Repository, TAIR)

???ui.leftmenu.abouttair???
	???ui.leftmenu.explanation???

???ui.leftmenu.bartitle???
	Repositories
	Author
	Title
	Date
	???ui.leftmenu.statisticschart???
	???ui.leftmenu.realtimefacts???
	???ui.leftmenu.trend???

???index.news???
	2019臺灣學術機構典藏研討會
	機構典藏系統RC7版本已發佈

???ui.leftmenu.copyrighttitle???
	???ui.leftmenu.copyrightpublisher???
	???ui.leftmenu.copyrightconference???

???ui.leftmenu.link???
	機構典藏計畫網站
	ROAR
	OpenDOAR
	SHERPA
	OAIster
	JAIRO
	Ira
	DSPACE
	RWWR
	臺大學術典藏NTU Scholars

"lin h i"???jsp.browse.items-by-author.description???

???jsp.browse.items-by-author.back???
???jsp.browse.items-by-author.order1???	???jsp.browse.items-by-author.order2???

Showing items 46-70 of 155 (7 Page(s) Totally)
<< < 1 2 3 4 5 6 7 > >>
View [10|25|50] records per page

Institution	Date	Title	Author
臺大學術典藏	2020-12-18T08:38:31Z	Catheter-related bacteraemia and infective endocarditis caused by Kocuria species	PO-REN HSUEH; Lin H.I.; Huang Y.T.; Chou C.H.; Liao C.H.; Wang C.Y.; Tan C.K.; Lin S.H.; Wang J.Y.; Lai C.C.; Lai C.C.;Wang J.Y.;Lin S.H.;Tan C.K.;Wang C.Y.;Liao C.H.;Chou C.H.;Huang Y.T.;Lin H.I.;Po-Ren Hsueh
臺大學術典藏	2020-12-09T01:38:20Z	A limb-girdle myopathy phenotype of RUNX2 mutation in a patient with cleidocranial dysplasia: A case study and literature review	Yang S.-H.; Lin H.-I.; Lin C.-H.; NI-CHUNG LEE; Hsueh S.-J.; Hsueh S.-J.;Ni-Chung Lee;Yang S.-H.;Lin H.-I.;Lin C.-H.
臺大學術典藏	2020-11-03T12:21:50Z	Mutational analysis of SYNJ1 gene (PARK20) in Parkinson's disease in a Taiwanese population	Chen K.-H.; Wu R.-M.; Lin H.-I.; CHUN-HWEI TAI; Lin C.-H.
臺大學術典藏	2020-11-03T12:21:49Z	Lack of RAB39B mutations in early-onset and familial Parkinson's disease in a Taiwanese cohort	Lin H.-H.;Wu R.-M.;Lin H.-I.;Chen M.-L.;Chun-Hwei Tai;Lin C.-H.; Lin H.-H.; Wu R.-M.; Lin H.-I.; Chen M.-L.; CHUN-HWEI TAI; Lin C.-H.
臺大學術典藏	2020-11-03T12:12:49Z	Lack of C9orf72 repeat expansion in Taiwanese patients with mixed neurodegenerative disorders	Chin-Hsien Lin;Chen T.-F.;Chiu M.-J.;Lin H.-I.;Wu R.-M.; CHIN-HSIEN LIN; Chen T.-F.; Chiu M.-J.; Lin H.-I.; Wu R.-M.
臺大學術典藏	2020-11-03T12:12:49Z	Vitamin D receptor genetic variants and Parkinson's disease in a Taiwanese population	Wu R.-M.; Lin H.-I.; Chen M.-L.; CHIN-HSIEN LIN; Chen K.-H.
臺大學術典藏	2020-11-03T12:12:49Z	The p.L302P mutation in the lysosomal enzyme gene SMPD1 is a risk factor for Parkinson disease.	CHIN-HSIEN LIN; Lin H.I.; Wu R.M.
臺大學術典藏	2020-11-03T12:12:47Z	COQ2 p.V393A variant, rs148156462, is not associated with Parkinson's disease in a Taiwanese population	CHIN-HSIEN LIN; Lin H.-I.; Chen M.-L.; Wu R.-M.; Chin-Hsien Lin;Lin H.-I.;Chen M.-L.;Wu R.-M.
臺大學術典藏	2020-11-03T12:12:46Z	Lack of CHCHD2 mutations in Parkinson's disease in a Taiwanese population	Fan T.-S.; Lin H.-I.; CHIN-HSIEN LIN; Wu R.-M.
臺大學術典藏	2020-11-03T12:12:44Z	Lovastatin protects neurite degeneration in LRRK2-G2019S parkinsonism through activating the Akt/Nrf pathway and inhibiting GSK3β activity	Chien C.-T.; Wu R.-M.; CHIN-HSIEN LIN; Lin H.-I.; Chen M.-L.; Lai T.-T.; Cao L.-P.; Farrer M.J.
臺大學術典藏	2020-11-03T12:12:43Z	Clinical heterogeneity of LRRK2 p.I2012T mutation	CHIN-HSIEN LIN; Lin H.-I.; Tai C.-H.; Chen C.-Y.; Chen M.-L.; Li H.-Y.; Lin Y.-H.; Chen T.-F.; Chen P.-L.; Wu R.-M.; Fan T.-S.
臺大學術典藏	2020-11-03T12:12:42Z	Lack of RAB39B mutations in early-onset and familial Parkinson's disease in a Taiwanese cohort	CHIN-HSIEN LIN; Tai C.-H.; Chen M.-L.; Lin H.-I.; Wu R.-M.; Lin H.-H.; Lin H.-H.;Wu R.-M.;Lin H.-I.;Chen M.-L.;Tai C.-H.;Chin-Hsien Lin
臺大學術典藏	2020-11-03T12:12:41Z	Lack of TMEM230 mutations in patients with familial and sporadic Parkinson's disease in a Taiwanese population	CHIN-HSIEN LIN; Lin H.-I.; Chen M.-L.; Wu R.-M.; Fan T.-S.; Fan T.-S.;Chin-Hsien Lin;Lin H.-I.;Chen M.-L.;Wu R.-M.
臺大學術典藏	2020-11-03T12:12:40Z	Generation of 2 induced pluripotent stem cell lines derived from patients with Parkinson's disease carrying LRRK2 G2385R variant	Hsieh P.C.H.; CHIN-HSIEN LIN; Lin H.-I.; Lu H.-E.; Syu S.-H.; Hsu Y.-H.; Ho M.-C.; Huang C.-Y.; Cheng Y.-C.; Cheng Y.-C.;Huang C.-Y.;Ho M.-C.;Hsu Y.-H.;Syu S.-H.;Lu H.-E.;Lin H.-I.;Chin-Hsien Lin;Hsieh P.C.H.
臺大學術典藏	2020-11-03T12:12:40Z	Depression and Catechol-O-methyltransferase (COMT) genetic variants are associated with pain in Parkinson's disease	Rizos A.; Chang C.-W.; Lin H.-I.; Wu Y.-R.; Ko C.-I.; Fan J.-Y.; Chaudhuri K.R.; CHIN-HSIEN LIN; Chin-Hsien Lin;Chaudhuri K.R.;Fan J.-Y.;Ko C.-I.;Rizos A.;Chang C.-W.;Lin H.-I.;Wu Y.-R.
臺大學術典藏	2020-11-03T12:12:39Z	Catechol-O-methyltransferase (COMT) genetic variants are associated with cognitive decline in patients with Parkinson's disease	Chin-Hsien Lin;Fan J.-Y.;Lin H.-I.;Chang C.-W.;Wu Y.-R.; CHIN-HSIEN LIN; Fan J.-Y.; Lin H.-I.; Chang C.-W.; Wu Y.-R.
臺大學術典藏	2020-11-03T12:12:39Z	PDE8B mutation is not associated with Parkinson's disease in a Taiwanese population	CHIN-HSIEN LIN; Fan T.-S.;Wu R.-M.;Lin H.-I.;Cheng C.;Chin-Hsien Lin; Fan T.-S.; Wu R.-M.; Lin H.-I.; Cheng C.
臺大學術典藏	2020-11-03T12:12:38Z	Generation of induced pluripotent stem cells (IBMSi011-A) from a patient with Parkinson's disease carrying LRRK2 p.I1371V mutation	Lin H.-I.;Cheng Y.-C.;Ko H.-W.;Wen C.-H.;Lu H.-E.;Huang C.-Y.;Hsieh P.C.H.;Chin-Hsien Lin; Lin H.-I.; Cheng Y.-C.; Ko H.-W.; Wen C.-H.; Lu H.-E.; Huang C.-Y.; Hsieh P.C.H.; CHIN-HSIEN LIN
臺大學術典藏	2020-11-03T12:12:38Z	Reprogramming of a human induced pluripotent stem cell (iPSC) line (IBMSi012-A) from an early-onset Parkinson's disease patient harboring a homozygous p.D331Y mutation in the PLA2G6 gene	Cheng Y.-C.;Lin H.-I.;Syu S.-H.;Lu H.-E.;Huang C.-Y.;Chin-Hsien Lin;Hsieh P.C.H.; Cheng Y.-C.; Lin H.-I.; Syu S.-H.; Hsieh P.C.H.; Lu H.-E.; Huang C.-Y.; CHIN-HSIEN LIN
臺大學術典藏	2020-11-03T12:12:38Z	A clinical and genetic study of early-onset and familial parkinsonism in taiwan: An integrated approach combining gene dosage analysis and next-generation sequencing	Wu R.-M.; Chen M.-L.; Chin-Hsien Lin;Chen P.-L.;Tai C.-H.;Lin H.-I.;Chen C.-S.;Chen M.-L.;Wu R.-M.; CHIN-HSIEN LIN; Chen P.-L.; Tai C.-H.; Lin H.-I.; Chen C.-S.
臺大學術典藏	2020-11-03T12:12:37Z	Craniocervical dystonia with levodopa-responsive parkinsonism co-segregating with a pathogenic ANO3 mutation in a Taiwanese family	Kuo M.-C.;Lin H.-I.;Chin-Hsien Lin; Kuo M.-C.; Lin H.-I.; CHIN-HSIEN LIN
臺大學術典藏	2020-11-03T11:57:07Z	Lack of C9orf72 repeat expansion in Taiwanese patients with mixed neurodegenerative disorders	Lin C.-H.;Chen T.-F.;MING-JANG CHIU;Lin H.-I.;Wu R.-M.; Lin C.-H.; Chen T.-F.; MING-JANG CHIU; Lin H.-I.; Wu R.-M.
臺大學術典藏	2020-09-28T07:04:52Z	Risk of colorectal cancer in type 2 diabetic patients: A population-based cohort study	Chao T.-T.; Wang J.-Y.; Lai C.-C.; Wang C.-Y.; Wang S.-M.; Lin H.-I.; Tang S.-H.; Lin H.-W.
臺大學術典藏	2020-08-13T05:24:24Z	Catheter-related bacteraemia and infective endocarditis caused by Kocuria species	Tan C.K.; Lin S.H.; JANN-YUAN WANG; Lai C.C.; Wang C.Y.; Liao C.H.; Chou C.H.; Huang Y.T.; Lin H.I.; Hsueh P.R.
臺大學術典藏	2020-08-12T07:46:56Z	Risk of sepsis among patients with COPD treated with fixed combinations of inhaled corticosteroids and long-acting Beta2 agonists	Chen C.-Y.; On the behalf of Taiwan Clinical Trial Consortium for Respiratory Diseases (TCORE); Lai C.-C.; HAO-CHIEN WANG; Chen L.; Yu C.-J.; Yu C.-J.; HAO-CHIEN WANG; Perng D.-W.; Cheng S.-L.; Hsu J.-Y.; Hsu W.-H.; Tsai Y.-H.; Hsiue T.-R.; Lin M.-C.; Lin H.-I.; Wang C.-Y.; Chang Y.-C.; Yang U.-C.; Chen C.-M.; Lin C.-S.; Chen L.; Wei Y.-F.; Chong I.-W.; Wang Y.-H.; Lin Y.S.; Wang C.-Y.; Wang C.-Y.;Lin Y.S.;Wang Y.-H.;Lai C.-C.;Hao-Chien Wang;Chen L.;Yu C.-J.;Yu C.-J.;Hao-Chien Wang;Perng D.-W.;Cheng S.-L.;Hsu J.-Y.;Hsu W.-H.;Tsai Y.-H.;Hsiue T.-R.;Lin M.-C.;Lin H.-I.;Wang C.-Y.;Chang Y.-C.;Yang U.-C.;Chen C.-M.;Lin C.-S.;Chen L.;Wei Y.-F.;Chong I.-W.;Chen C.-Y.;On The Behalf Of Taiwan Clinical Trial Consortium For Respiratory Diseases (Tcore)

Showing items 46-70 of 155 (7 Page(s) Totally)
<< < 1 2 3 4 5 6 7 > >>
View [10|25|50] records per page

	English \| 正體中文 \| 简体中文 \| 0
	???header.visitor??? : 52741614 ???header.onlineuser??? : 640 ???header.sponsordeclaration???